Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,015 positions on this site are linked to Height, out of 2,505,961 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

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Strength of the evidence: all 2+ 3+ 4 Connections: all only those linked to a condition, drug or sense

← Back to Height

Standard

Height

BRD4 · rs4809130

See detailed info → Standard

Height

VAMP3 · rs11576572

See detailed info → Standard

Height

near SNORD116 · rs6563779

See detailed info → Standard

Height

MED4 · rs4942747

See detailed info → Standard

Height

near RNU1-148P · rs980812

See detailed info → Standard

Height

near VN1R10P · rs9379978

See detailed info → Standard

Height

DAAM2 · rs913574

See detailed info → Standard

Height

near ARMC12 · rs7752049

See detailed info → Standard

Height

near LINC01968 · rs4320032

See detailed info → Standard

Height

near FENDRR · rs1918826

See detailed info → Standard

Height (baseline)

FAM83C · rs111916968

See detailed info → Standard

height (minimum, inv-normal transformed)

ZFAS1 · rs68014903

See detailed info → Standard

Height (baseline)

near MICA · rs62395268

See detailed info → Standard

Height

STARD4-AS1 · rs17133647

See detailed info → Standard

Height

near EXOC2 · rs11243102

See detailed info → Standard

Height

CSH2 · rs2854207

See detailed info → Standard

Height

CDK2AP1 · rs1879380

See detailed info → Standard

Height

near RPS19P6 · rs11793647

See detailed info → Standard

Height

PCMTD2 · rs6512309

See detailed info → Standard

Height (baseline)

WBP1L · rs2253709

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Showing 20 of 11015 · page 165 of 551

Questions about variants on this site

What is a "variant" page on this site?

One specific position in the genome (an rsID), explained in plain language with what published research has found it linked to, and how strong that link actually is.

Where does new variant data come from?

The public GWAS Catalog, checked every twenty minutes, plus variants added manually after research review. Every one passes the same quality gate before publishing.

Does being listed here mean a variant causes a condition?

No. Listing reflects an association from published research, not a diagnosis or a cause. Most common variants shift probability modestly rather than determining an outcome.

Can I search this list by gene or rsID?

Yes — the search box above matches gene symbols and rsIDs as well as trait names.